Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 585742Generated: October 25, 2026

2-Chloro-1-methylpyridinium iodide → (S)-4-(tert-butoxycarbonylamino)-N-(1-triphenylmethylpyrazolo[3,4-b]pyridin-4-yl)thiochromane-7-carboxamide

https://huagongshe.com/reaction/585742

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Chloro-1-methylpyridinium iodideHCID 167069—
Reactant4-Amino-1-triphenylmethylpyrazolo[3,4-b]pyridineHCID 22337470—
Reactant(S)-4-(tert-butoxycarbonylamino)thiochromane-7-carboxylic acidHCID 59089455—
Product(S)-4-(tert-butoxycarbonylamino)-N-(1-triphenylmethylpyrazolo[3,4-b]pyridin-4-yl)thiochromane-7-carboxamideHCID 6961962173.8%

Reaction Steps

By a similar reaction operation as in Starting Material Synthetic Example 53 using (S)-4-(tert-butoxycarbonylamino)thiochromane-7-carboxylic acid (500 mg), 4-amino-1-triphenylmethylpyrazolo[3,4-b]pyridine (670 mg) synthesized according to a known method and 2-chloro-1-methylpyridinium iodide (496 mg), the objective (S)-4-(tert-butoxycarbonylamino)-N-(1-triphenylmethylpyrazolo[3,4-b]pyridin-4-yl)thiochromane-7-carboxamide (796 mg) was obtained as a pale yellow amorphous solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06933305B2
Source datasetuspto-grants-2005_08
ORD IDord-96f348abe2ff423fb07d416f935fc79e
Source noteuspto-grants-2005_08