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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTert-butyl trans-3-amino-4-oxo-2-phenyl-2,3,4,5-tetrahydro-1,5-benzothiazepine-5-acetateHCID 13533191—
ReactantSuccinimido indolecarboxylateHCID 19993581—
SolventDimethylformamideHCID 6228—
ProductTert-butyl trans-3-(2-indolecarboxamido)-4-oxo-2-phenyl-2,3,4,5-tetrahydro-1,5-benzothiazepine-5-acetateHCID 1464856589.7%

Reaction Conditions

Temperature60 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05055464
Source datasetuspto-grants-1991_10
ORD IDord-0224101d289e4d839816eb7d9ee16979
Source noteuspto-grants-1991_10