HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 345154Generated: October 29, 2026
Tert-butyl trans-3-amino-4-oxo-2-phenyl-2,3,4,5-tetrahydro-1,5-benzothiazepine-5-acetate → Tert-butyl trans-3-(2-indolecarboxamido)-4-oxo-2-phenyl-2,3,4,5-tetrahydro-1,5-benzothiazepine-5-acetate
https://huagongshe.com/reaction/345154
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tert-butyl trans-3-amino-4-oxo-2-phenyl-2,3,4,5-tetrahydro-1,5-benzothiazepine-5-acetate | HCID 13533191 | — |
| Reactant | Succinimido indolecarboxylate | HCID 19993581 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Tert-butyl trans-3-(2-indolecarboxamido)-4-oxo-2-phenyl-2,3,4,5-tetrahydro-1,5-benzothiazepine-5-acetate | HCID 14648565 | 89.7% |
Reaction Steps
In 300 ml of dimethylformamide are dissolved 18 g of tert-butyl trans-3-amino-4-oxo-2-phenyl-2,3,4,5-tetrahydro-1,5-benzothiazepine-5-acetate and 12 g of succinimido indolecarboxylate as synthesized by a known method, and the solution is stirred at 60° C. for 33.5 hours. The reaction mixture is poured to ice-water, and the mixture is stirred to separate crystals, which are collected by filtration and washed with water and dried to give 22 g of tert-butyl trans-3-(2-indolecarboxamido)-4-oxo-2-phenyl-2,3,4,5-tetrahydro-1,5-benzothiazepine-5-acetate, m.p. 196°-200° C. (decomposition).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05055464 |
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| Source dataset | uspto-grants-1991_10 |
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| ORD ID | ord-0224101d289e4d839816eb7d9ee16979 |
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| Source note | uspto-grants-1991_10 |
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