HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1809763Generated: October 27, 2026
Tert-butyl (2-amino-2-(3-chlorophenyl)ethyl)carbamate → HCID 178453676, compound
https://huagongshe.com/reaction/1809763
Participants
| Role | Name | HCID | Charge |
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| Reactant | Tert-butyl (2-amino-2-(3-chlorophenyl)ethyl)carbamate | HCID 69108731 | — |
| Reactant | HCID 178504618 | HCID 178504618 | — |
| Product | HCID 178453676 | HCID 178453676 | — |
Reaction Steps
The mixture of {4-[3-(2-methanesulfinyl-pyrimidin-4-yl)-1H-pyrazolo[3,4-d]pyrimidin-6-ylamino]-cyclohexyl}-carbamic acid tert-butyl ester (from Example 9 supra) (300 mg, 0.64 mmol) and [2-amino-2-(3-chloro-phenyl)-ethyl]-carbamic acid tert-butyl ester (from Example 4 supra) (686 mg, 2.5 mmol) was heated at 130° C. with stirring for 2 hours. The resulting oil was purified by chromatography (silica gel, 8 g, 200-300 mesh, eluting with dichloromethane:methanol, 50:1 to 30:1) to afford crude [4-(3-{2-[2-tert-butoxycarbonylamino-1-(3-chloro-phenyl)-ethylamino]-pyrimidin-4-yl}-1H-pyrazolo[3,4-d]pyrimidin-6-ylamino)-cyclohexyl]-carbamic acid tert-butyl ester. (Yield 140 mg, 32.5%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08362023B2 |
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| Source dataset | uspto-grants-2013_01 |
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| ORD ID | ord-b21e5bf1f8994a4ca019e64cee879dd9 |
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| Source note | uspto-grants-2013_01 |
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